Mondoxyne NL 100mg
Monodoxyne NL 100mg
Approved
Approval ID
1f80aef4-3ca9-42ec-e054-00144ff8d46c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 11, 2015
Manufacturers
FDA
Oculus Innovative Sciences
DUNS: 081642964
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Doxycycline
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69668-433
Application NumberANDA204446
Product Classification
M
Marketing Category
C73584
G
Generic Name
Doxycycline
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 11, 2015
FDA Product Classification
INGREDIENTS (1)
DOXYCYCLINEActive
Quantity: 100 mg in 100 mg
Code: N12000U13O
Classification: ACTIM